EP1931633A2 - Derives de 3-azabicyclo[3.1.0]hexane en tant qu'inhibiteurs de la dipeptidyl peptidase-iv - Google Patents

Derives de 3-azabicyclo[3.1.0]hexane en tant qu'inhibiteurs de la dipeptidyl peptidase-iv

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Publication number
EP1931633A2
EP1931633A2 EP06820744A EP06820744A EP1931633A2 EP 1931633 A2 EP1931633 A2 EP 1931633A2 EP 06820744 A EP06820744 A EP 06820744A EP 06820744 A EP06820744 A EP 06820744A EP 1931633 A2 EP1931633 A2 EP 1931633A2
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EP
European Patent Office
Prior art keywords
compound
azabicyclo
hex
carbonitrile
glycyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Application number
EP06820744A
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German (de)
English (en)
Inventor
Jitendra A. Sattigeri
Murugaiah M S Andappan
Kaushal Kishore
Sachin Sethi
Sachin Ramesh Kandalkar
Chanchal Kumar Pal
Dipak C. Mahajan
Shahadat Ahmed
Santhosh Sadashiv Parkale
T Srinivasan
Lalima Sharma
Vinay S. Bansal
Anita Chugh
Joseph Alexanand Davis
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Ranbaxy Laboratories Ltd
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Ranbaxy Laboratories Ltd
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Publication of EP1931633A2 publication Critical patent/EP1931633A2/fr
Withdrawn legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/52—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring condensed with a ring other than six-membered
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Definitions

  • the present invention relates to 3-azabicyclo[3.1.0]hexane derivatives as dipeptidyl peptidase-IV inhibitors and the processes for the synthesis of the compounds.
  • This invention also relates to pharmacological compositions containing the compounds of the present invention, and methods of treating diabetes, especially type 2 diabetes, as well as prediabetes, diabetic dyslipidemia, metabolic acidosis, ketosis, satiety disorders, and obesity.
  • These inhibitors can also be used to treat conditions manifested by a variety of metabolic, neurological, anti-inflammatory, and autoimmune disorders like inflammatory disease, multiple sclerosis, rheumatoid arthritis; viral, cancer and gastrointestinal disorders.
  • the compounds of this invention can also be used for treatment of infertility arising due to polycystic ovary syndrome.
  • Type 2 diabetes mellitus also known as "non-insulin dependent diabetes mellitus” (NIDDM)
  • NIDDM non-insulin dependent diabetes mellitus
  • Type 2 diabetes is a complex metabolic disorder, characterized by hyperglycemia and hyperinsulinemia. This results from contribution of impaired insulin secretion from ⁇ -cells in pancreas and insulin resistance mainly in muscle and liver.
  • the insulin resistant individuals in addition to being hyperglycemic, exhibit a constellation of closely related clinical indications, which include obesity, hypertension and dyslipidemia.
  • Uncontrolled hyperglycemia can further lead to late stage microvascular and macrovascular complications such as nephropathy, neuropathy, retinopathy and premature atherosclerosis.
  • ASCVD atherosclerotic cardiovascular disease
  • NIDDM neurode-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide-derived neuropeptide.
  • biguanides which lower hepatic glucose production (e. g., metformin)
  • ⁇ -glucosidase inhibitors which delay intestinal absorption of carbohydrates [e.g., acarbose] ⁇ Lancet, 2005, 365, 1333-1346).
  • the insulin sensitizers like pioglitazone and rosiglitazone (TZDs), which exhibit their effect by PPAR ⁇ agonism, control hyperglycaemia by improving peripheral insulin sensitivity without increasing circulating insulin levels.
  • all these agents are associated with one or more of side effects like hypoglycaemia, gastrointestinal side effects including abdominal discomfort, bloating, flatulence, hepatotoxicity, weight gain, dilutional anemia and peripheral edema ⁇ Endocrine Rev., 2000, 2L, 585-618).
  • side effects like hypoglycaemia, gastrointestinal side effects including abdominal discomfort, bloating, flatulence, hepatotoxicity, weight gain, dilutional anemia and peripheral edema ⁇ Endocrine Rev., 2000, 2L, 585-618.
  • NIDDM rosiglitazone
  • the safe and, preferably, orally bioavailable therapeutic agents that would accelerate glucose clearance by stimulating endogenous insulin secretion in a glucose-dependent manner, free from hypoglycemic episodes
  • GLP-I incretin-secreting hormones
  • GLP-I glucose-dependent insulinotropic polypeptide
  • GLP-I (7-36) is a 29 amino acid containing peptide derived by post translational processing of proglucagon in the L-cells of the distal small intestine in response to the food intake.
  • DPP IV dipeptidyl peptidase-IV
  • GLP-I 9-36
  • GIP GIP
  • DPP IV inhibition leads to an increase of biologically active forms of both GLP-I and GIP to therapeutically beneficial levels and thus enhances the body's own normal homeostatic mechanism. As the incretins are released by the body, only in response to the food intake, DPP IV inhibition is not expected to increase the level of insulin at inappropriate times, such as in between meals, which can otherwise lead to hypoglycemia.
  • the initial proof of concept for DPP IV-based therapy has been obtained from DPP IV knockout (KO) mice and other preclinical animal models.
  • DPP IV KO rat and mice have shown normal glucose tolerance and didn't develop diabetic symptoms, even when fed with fat-rich food.
  • Clinical and pre-clinical studies with DPP IV-resistant GLP-I analogs like Exenatide have provided indirect but valuable additional validation for the DPP IV target.
  • an early DPP IV inhibitor viz., ⁇ VP DPP 728
  • significant improvement in mean 24 hours glucose excursion with lower insulin, glucagon and HbAIc levels were observed in the treated patients.
  • the experimental evidence suggests that DPP IV inhibition offers an added benefit in preservation and regeneration of ⁇ cells.
  • DPP IV inhibitors may thus be used in disease modifying therapy in type 1 and late-stage type 2 diabetes.
  • the DPP IV inhibitors may also manifest the beneficial effect of delaying gastric emptying observed with GLP-I. This is corroborated by recent Phase II studies, which demonstrate that no body weight gain was observed with DPP IV inhibitors during the treatment period of the patients with diabetes and obesity (Current Opin. Pharma., 2004, 4, 589-596).
  • the present invention provides inhibitors and methods for treating conditions mediated by DPP IV, like diabetes, especially, type 2 diabetes mellitus, as well as prediabetes, diabetic dyslipidemia, metabolic acidosis, ketosis, satiety disorders, and obesity. These inhibitors can also be used to treat conditions manifested by a variety of metabolic ⁇ Expert Opin.
  • Investig. Drug, 2003, Yl, 87-100 neurological (Brain Res., 2005, 1048, 177-184), anti-inflammatory, and autoimmune disorders (Clin. Diagnostic Lab. Immunol 2002, 9, 1253-1259) like inflammatory disease, multiple sclerosis, rheumatoid arthritis (Clin. Immunol. Immunopatk, 1996, 80, 31-37); viral (Clin. Immunol., 1999, 91,, 283-295), cancer (Cancer Res., 2005, 65, 1325-1334), blood disorders (Blood, 2003, 102, 1641-1648) and gastrointestinal disorders.
  • the compounds of this invention can also be used for treatment of infertility arising due to polycystic ovary syndrome.
  • WO04/009544 discloses 2-cyano-4-fluoropyrrolidine derivative or its salts.
  • WO03/106456 discloses novel compounds possessing dipeptidyl peptidase-IV enzyme inhibitory activity.
  • WO03/074500 discloses new compounds, which contain fluorine atoms and are DPP-IV enzyme inhibitors.
  • WO 03/02553 discloses fluoropyrrolidines as dipeptidyl peptidase inhibitors.
  • WO03/037327 discloses N-(substituted)pyrrolidine derivatives as dipeptidyl peptidase-IV inhibitors.
  • WO03/057666 discloses novel inhibitors of dipeptidyl peptidase-IV.
  • WO01/055105 discloses N-(substituted)-2-cyanopyroles and pyrrolines, which are inhibitors of the enzyme DPP-IV.
  • US6011155 discloses N- (substituted glycyl)-2-cyanopyrrolidines, pharmaceutical compositions containing them and their use in inhibiting dipeptidyl peptidase-IV.
  • the compound (2iS)-l-[[(3-hydroxy-l- adamantyl)amino]acetyl]-2-cyanopyrrolidine [vildagliptin] has been disclosed as a potent, selective, and orally bioavailable dipeptidyl peptidase-IV inhibitor with antihyperglycemic properties vide reference J. Med. Chem., 2003, 46(13), 2774-2789.
  • 3-azabicyclo[3.1.0]hexane derivatives possessing dipeptidylpeptidase-IV enzyme inhibitory activity are also provided. Also provided are processes for synthesizing such compounds.
  • These compounds can be used in treatment of conditions mediated by DPP IV, like diabetes, especially, type 2 diabetes mellitus as well as pre-diabetes, diabetic dyslipidemia, metabolic acidosis, ketosis, satiety disorders, and obesity.
  • DPP IV can be used for treating conditions manifested by a variety of metabolic, neurological, anti-inflammatory, and autoimmune disorders like inflammatory disease, multiple sclerosis, rheumatoid arthritis viral, cancer and gastrointestinal disorders.
  • the compounds of this invention can also be used for treatment of infertility arising due to polycystic ovary syndrome.
  • compositions containing such compounds are provided together with the pharmaceutically acceptable carriers or diluents, which can be used for the treatment of dipeptidyl peptidase-IV mediated pathologies.
  • These pharmaceutical compositions may be administered or coadministered by a wide variety of routes including, for example, oral or parenteral.
  • the composition may also be administered or coadministered in slow release dosage forms.
  • racemates, enantiomers, diastereomers, N-oxides, polymorphs, pharmaceutically acceptable salts and pharmaceutically acceptable solvates of these compounds, prodrugs and metabolites, having the same type of activity are also provided as well as pharmaceutical compositions comprising the compounds, their metabolites, racemates, enantiomers, N-oxides, polymorphs, solvates, prodrugs or pharmaceutically acceptable salts thereof, in combination with a pharmaceutically acceptable carrier and optionally included excipients.
  • A can be selected from
  • T can be cyano, halogen, alkyl, alkenyl, alkynyl, hydroxy, alkoxy, carbonyl, thiocarbonyl, and oxo and n is 0-3;
  • W is -C(R x Ry) n -, wherein n is an integer of 1 to 3 and R x and R y can be independently selected from hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl or heterocyclyl;
  • R comprises one of the following Formulas:
  • X can be no atom, -CO-, -CS-, -C(R x R y )i- or -SO 2 -, wherein 1 is an integer of 1-3; and R x and R y are defined as above;
  • Y can be no atom, -O- or -NR x -, with the proviso that Y cannot be -O- or -NR x - when X is C(R x Ry)i [wherein 1 is an integer of I]; Z is alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl or heterocyclyl; R 3 is hydrogen, alkyl or aryl; and R' is R x , -CN, carboxy, halogen, carbonyl, or amino.
  • the invention relates to compounds of general Formula Ia,
  • the invention relates to compounds of general Formula Ib,
  • formula Ib including pharmaceutically acceptable salts, pharmaceutically acceptable solvates, enantiomers, diastereomers, polymorphs, prodrugs, metabolites or N-oxides thereof, wherein A, W, Ra, R', X, Y and Z are defined as above.
  • the invention relates to compounds of general Formula Ic, formula Ic including pharmaceutically acceptable salts, pharmaceutically acceptable solvates, enantiomers, diastereomers, polymorphs, prodrugs, metabolites or N-oxides thereof, wherein A, W, R a , R', R x , R y , X, Y and Z are defined as above.
  • the invention encompasses compounds that include, for example,
  • the present invention relates to the therapeutically effective dose of a compound of Formula 1 alone or in combination with one or more of other therapeutic agents used for treating metabolic disorder or related diseases.
  • therapeutic agents include, but are not limited to, 1) antihyperglycemic agents (a) other DPP IV inhibitors, e.g., saxagliptin, (b) insulin sensitizers, (I) PPAR agonists, for example, PP AR ⁇ agonists (e.g., rosiglitazone and pioglitazone), (II) PPAR ⁇ / ⁇ dual agonists (e.g., tesaglitazar and muraglitazar), and (III) PPAR pan-agonists (e.g., GSK 667954) (c) biguanides, e.g., metformin, (d) insulin secretagogues, for example, sulphonyl ureas (e.g., glimeperide) and
  • PSN105 inhibitors of 11/3- hydroxysteroid dehydrogenase type 1, (i) glucagon receptor antagonists, (j) GLP-I and GLP-I receptor agonists, e.g. liraglutide (Ic) insulin or insulin mimetics, (1) GIP and GIP receptor agonists (m) PACAP and PACAP receptor agonists, (n) fructose 1,6 bisphosphatase inhibitors; (o) glucose 6 phosphates inhibitors; (p) Sodium glucose transporter 2 (SGLT2) inhibitor, e.g., Kissei - 869682; (q) AMP-Activated protein kinase activators;
  • HMG-CoA reductase inhibitors e.g., atorvastatin, simvastatin, and fluvastatin
  • sequestrants cholestyramine, colestipol, and dialkylaminoalkyl derivatives of a cross-linked dextran
  • nicotinyl alcohol, nicotinic acid or a salt thereof e.g., ⁇ - sitosterol and ezetimibe
  • acyl CoA:cholesterol acyltransferase inhibitors e.g., avasimibe
  • CETP inhibitors e.g., torcetrapib
  • CBl receptor inverse agonists and antagonists e.g., rimonabant
  • melanocortin-receptor agonists in particular, melanocortin-4 receptor agonists
  • ghrelin antagonists in particular, melanocortin-4 receptor agonists
  • neuropeptide Yi or Y 5 antagonists in particular, melanin-concentrating hormone (MCH) receptor antagonists and (vii) fenfluramine, dexfenfluramine, phentermine, sibutramine, orlistat, and the like;
  • antihypertensive agents (i) ACE inhibitors, e.g., enalapril, lisinopril, and quinapril, (ii) angiotensin II receptor antagonists and agonists, e.g., losartan, candesartan, irbesartan, valsartan, and eprosartan, (iii) /3-blockers, and (iv) calcium channel blockers; and
  • anti-TNF agent or c-AMP raising agents such as, for example, PDE inhibitors.
  • alkyl refers to a monoradical branched or unbranched saturated hydrocarbon chain having from 1 to 20 carbon atoms.
  • This term can be exemplified by groups such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec- butyl, t-butyl, n-pentyl, isopentyl, neopentyl, n-hexyl, n-decyl, tetradecyl, and the like.
  • R x and R x are independently selected from hydrogen, halogen, hydroxy, alkyl, alkenyl, alkynyl, alkenyl, alkoxy, cycloalkyl, cycloalkenyl, aryl, aralkyl, heterocyclyl, heteroaryl, heterocyclylalkyl, heteroarylallcyl or carboxy ⁇ , nitro or -
  • m is an integer from 0-2 and R ⁇ is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, aralkyl, aryl, heterocyclyl, heteroaryl, heteroarylallcyl or heterocyclylalkyl).
  • alkenyl refers to a monoradical of a branched or unbranched unsaturated hydrocarbon group having from 2 to 20 carbon atoms with cis, trans or geminal geometry.
  • Alkenyl groups can be optionally interrupted by atom(s) or group(s) independently chosen from oxygen, sulfur, phenylene, sulphinyl, sulphonyl and -NR ⁇ - (wherein R 0 is the same as defined earlier). In the event that alkenyl is attached to a heteroatom, the double bond cannot be alpha to the heteroatom.
  • alkynyl refers to a monoradical of an unsaturated hydrocarbon, having from 2 to 20 carbon atoms.
  • Alkynyl groups can be optionally interrupted by atom(s) or group(s) independently chosen from oxygen, sulfur, phenylene, sulphinyl, sulphonyl and -NR 0 - (wherein R 0 is the same as defined earlier). In the event that alkynyl groups are attached to a heteroatom, the triple bond cannot be alpha to the heteroatom.
  • cycloalkyl refers to cyclic alkyl groups of from 3 to 20 carbon atoms having a single cyclic ring or multiple condensed rings, which may optionally contain one or more olefinic bonds, unless otherwise constrained by the definition.
  • Such cycloalkyl groups can include, for example, single ring structures, including cyclopropyl, cyclobutyl, cyclooctyl, cyclopentenyl, and the like or multiple ring structures, including adamantanyl, and bicyclo [2.2.1] heptane or cyclic alkyl groups to which is fused an aryl group, for example, indane, and the like.
  • cycloalkyl substituents optionally may be substituted further by 1-3 substituents selected from alkyl, alkenyl, alkynyl, carboxy, hydroxy, alkoxy, halogen, CF 3 , -NR x R 7T , - R ⁇ , R ⁇ , m and R 1 ⁇ are the same as defined earlier).
  • Cycloalkylalkyl refers to alkyl-cycloalkyl group linked through alkyl portion, wherein the alkyl and cycloalkyl are the same as defined earlier.
  • aryl refers to aromatic system having 6 to 14 carbon atoms, wherein the ring system can be mono-, bi- or tricyclic and are carbocyclic aromatic groups.
  • halogen e.
  • Aryl groups optionally may be fused with a cycloalkyl group, wherein the cycloalkyl group may optionally contain heteroatoms selected from O, N or S.
  • Groups such as phenyl, naphthyl, anthryl, biphenyl, and the like exemplify this term.
  • the substituents are attached to a ring atom, i.e., carbon or heteroatom in the ring.
  • heteroaryl groups include oxazolyl, imidazolyl, pyrrolyl, 1,2,3-triazolyl, 1,2,4-triazolyl, tetrazolyl, thiazolyl, oxadiazolyl, benzoimidazolyl, thiadiazolyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, thienyl, isoxazolyl, triazinyl, furanyl, benzofuranyl, indolyl, benzthiazinyl, benzthiazinonyl, benzoxazinyl, benzoxazinonyl, quinazonyl, carbazolyl phenothiazinyl, phenoxazinyl, benzothiazolyl or be
  • Heterocyclyl can optionally include rings having one or more double bonds. Such ring systems can be mono-, bi- or tricyclic. Carbonyl or sulfonyl group can replace carbon atom(s) of heterocyclyl. Unless otherwise constrained by the definition, the substituents are attached to the ring atom, i.e., carbon or heteroatom in the ring. Also, unless otherwise constrained by the definition, the heterocyclyl ring optionally may contain one or more olefinic bond(s).
  • heterocyclyl groups include oxazolidinyl, tetrahydroruranyl, dihydrofuranyl, benzoxazinyl, benzthiazinyl, imidazolyl, benzimidazolyl, tetrazolyl, carbaxolyl, indolyl, phenoxazinyl, phenothiazinyl, dihydropyridinyl, dihydroisoxazolyl, dihydrobenzofuryl, azabicyclohexyl, thiazolidinyl, dihydroindolyl, pyridinyl, isoindole 1,3-dione, piperidinyl, tetrahydropyranyl, piperazinyl, 3H-imidazo[4,5-b]pyridine, isoquinolinyl, IH- pyrrolo[2,3-b]pyridine or piperazinyl and the like.
  • amino refers to group -N(Rk) 2 , (wherein each R ⁇ is independently selected from hydrogen, alkyl, cycloalkyl, aryl, heteroaryl, heterocyclyl).
  • halogen refers to -F, -Cl, -Br, and -I.
  • leaving group refers to groups that exhibit or potentially exhibit the properties of being labile under the synthetic conditions and also, of being readily separated from synthetic products under defined conditions. Examples of leaving groups include, but are not limited to, halogen (e.g., F, Cl, Br, I), triflates, tosylate, mesylates, alkoxy, thioalkoxy, or hydroxy radicals and the like.
  • protecting groups refers to moieties that prevent chemical reaction at a location of a molecule intended to be left unaffected during chemical modification of such molecule.
  • protecting groups may be used on groups, such as hydroxy, amino, or carboxy. Examples of protecting groups are found in T. W. Greene and P.G.M. Wuts, "Protective Groups in Organic Synthesis", 2 nd Ed., John Wiley and Sons, New York, N.Y., which is incorporated herein by reference.
  • the species of the carboxylic protecting groups, amino protecting groups or hydroxy protecting groups employed are not critical, as long as the derivatised moieties/moiety is/are stable to conditions of subsequent reactions and can be removed without disrupting the remainder of the molecule.
  • pharmaceutically acceptable salts refers to derivatives of compounds that can be modified by forming their corresponding acid or base salts.
  • examples of pharmaceutically acceptable salts include, but are not limited to, mineral or organic acids salts of basic residues (such as amines), or alkali or organic salts of acidic residues (such as carboxylic acids), and the like.
  • pharmaceutically acceptable salts also refers to a salt prepared from pharmaceutically acceptable non-toxic inorganic or organic acid. Examples of such inorganic acids include, but are not limited to, hydrochloric, hydrobromic, hydroiodic, nitrous, nitric, carbonic, sulfuric, phosphoric acid, and the like.
  • organic acids include, but are not limited to aliphatic, cycloaliphatic, aromatic, heterocyclic, carboxylic and sulfonic classes of organic acids, for example, formic, acetic, propionic, succinic, glycolic, gluconic, lactic, malic, tartaric, citric, ascorbic, glucuronic, maleic, fumaric, pyruvic, aspartic, glutamic, benzoic, anthranilic, mesylic, salicylic, p-hydroxybenzoic, phenylacetic, mandelic, embonic, methanesulfonic, ethanesulfonic, benzenesulfonic, panthenic, toluenesulfonic, 2- hydroxyethanesulfonic acid and the like.
  • solvates refers to solvates with water (i.e., hydrates) or pharmaceutically acceptable solvents, for example, ethanol and the like. Such solvates are also encompassed within the scope of the disclosure. Furthermore, some of the crystalline forms for compounds described herein may exist as polymorphs and as such are intended to be included in the scope of the disclosure.
  • the present invention within its scope also includes prodrugs of the disclosed compounds of Formula I.
  • prodrugs will be functional derivatives of these compounds, which are readily convertible in vivo into the active drugs.
  • Conventional procedure for the selection and preparation of suitable prodrug derivatives are described, for example, in “Targeted prodrug design to optimize drug delivery", AAPS PharmSci. (2000), 2(1), E6. Detailed Description of the Invention
  • the compounds disclosed herein may be prepared by techniques well known in the art and familiar to the skilled synthetic organic chemist.
  • the compounds of the present invention may be prepared by the following reaction sequences as depicted in, for example, Schemes I, II, III, IV and V.
  • the compounds of Formula VI can be prepared, for example, following Scheme I.
  • Path a A compound of Formula II (wherein P is an amino protecting group, for example, ⁇ -butyl carbamate (Boc), 9-fluorenylmethyl carbamate (Fmoc), allyloxycarbonyl or benzyl derivative; E is -(CH 2 ) m - and m is OrI) can be reacted with a compound of Formula III (wherein L is a leaving group such as halide or hydroxy; X is no atom, -CO-, - SO 2 - or -CH 2 -; Y is O or no atom; and Z is alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl or heterocyclyl) to give the compound of Formula Va.
  • Path b The compound of Formula II can be reacted with a compound of Formula III (wherein P is an amino protecting group, for example, ⁇ -butyl carbamate (Boc), 9-fluorenylmethyl
  • the reaction of the compound of Formula II with the compound of Formula III (wherein X is -CO-, -SO 2- or -CH 2 - and Y is -O- or no atom) to give the compound of Formula Va (Path a) can be carried out in a solvent, for example, dichloromethane, toluene, dichloroethane, tetrahydrofuran, ether or dioxane, in the presence of a base, for example, triethylamine, N,N-diisopropylethylamine or N-methylmorpholine at a temperature of 0 to 100 0 C.
  • a solvent for example, dichloromethane, toluene, dichloroethane, tetrahydrofuran, ether or dioxane
  • a base for example, triethylamine, N,N-diisopropylethylamine or N-methylmorpholine at a temperature of 0 to
  • reaction of the compound of Formula II with the compound of Formula III (wherein X and Y are no atom) to give the compound of Formula Va (Path a) can be carried out in a solvent, for example, dimethylformamide, dioxane, tetrahydrofuran or dimethylsulphoxide, in the presence of a base, for example, potassium carbonate, triethylamine or N,N-diisopropylethylamine at a temperature of 0 to 150 0 C.
  • a solvent for example, dimethylformamide, dioxane, tetrahydrofuran or dimethylsulphoxide
  • a base for example, potassium carbonate, triethylamine or N,N-diisopropylethylamine at a temperature of 0 to 150 0 C.
  • reaction of the compound of Formula II with the compound of Formula IV to give a compound of Formula Vb can be carried out in a solvent, for example, dichloromethane, toluene, dichloroethane, tetrahydrofuran, ether or dioxane, optionally, in the presence of a base, for example, potassium carbonate, triethylamine, diisopropylethylamine or N-methylmorpholine.
  • a solvent for example, dichloromethane, toluene, dichloroethane, tetrahydrofuran, ether or dioxane
  • a base for example, potassium carbonate, triethylamine, diisopropylethylamine or N-methylmorpholine.
  • the deprotection of the compound of Formula Va an4 Formula Vb to form the compound of Formula VI can be carried out in the presence of />-toluenesulphonic acid, trifluoroacetic acid or piperidine in a solvent, for example, acetonitrile, tetrahydrofuran or dioxane, dimethylformamide or a mixture thereof.
  • a solvent for example, acetonitrile, tetrahydrofuran or dioxane, dimethylformamide or a mixture thereof.
  • the deprotection can also be carried out by other deprotection methods known to a skilled organic chemist.
  • the compound of Formula IX can be prepared, for example, following Scheme II.
  • the compound of Formula VI can be reacted with a compound of Formula VTI (wherein P is an amino protecting group and W is -C(R x Ry) n -, wherein n is an integer of 1 to 3 and R x and R y can be independently selected from hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl or heterocyclyl) to form a compound of Formula VIII, which can be deprotected to give a compound of Formula IX.
  • a compound of Formula VTI wherein P is an amino protecting group and W is -C(R x Ry) n -, wherein n is an integer of 1 to 3 and R x and R y can be independently selected from hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl or heterocyclyl
  • the reaction of the compound of Formula VI with a compound of Formula VTI to give a compound of Formula VIII can be carried out in a solvent, for example, tetrahydrofuran, dimethylformamide or dioxane using a coupling agent, for example, 1,3- dicyclohexylcarbodiimide (DCC), 1 -ethyl-3-(3 '-dimethylaminopropyl)carbodiimide hydrochloride (EDCI), N-[(dimethylamino)- IH- 1 ,2,3 -triazolo[4,5-£>]pyridylmethylene]-N- methylmethanaminium hexafluorophosphate N-oxide ( ⁇ ATU) or benzotriazol-1-yl-N- oxy-tris(pyrrolidino)phosphonium hexafluorophosphate (PyBOP) and, optionally, a catalyst, for example, 1-hydroxybenzotriazole ( ⁇ OB
  • Path c The compound of Formula X (wherein A can be selected from
  • T can be cyano, halogen, alkyl, alkenyl, alkynyl, hydroxy, alkoxy, carbonyl, thiocarbonyl, and oxo and n is 0-3, W is -C(R x Ry) n -, wherein n is an integer of 1 to 3 and R x and R y can be independently selected from hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heteroaryl or heterocyclyl and L is a leaving group) is reacted with a compound of Formula VI to form a compound of Formula XI.
  • Path d The compound of Formula X (wherein A, W and L are defined as earlier) is reacted with a compound of Formula IX to form a compound of Formula XII.
  • the above reactions can be carried out in a solvent, for example, dimethyl formamide, tetrahydrofuran, dioxane, diethyl ether, dichloromethane, toluene or dichloroethene and a base, for example, potassium carbonate, triethylamine, N,N-diisopropylethylamine or N-methylmorpholine, optionally in the presence of a catalyst, like sodium iodide and tetra-n-butylammonium iodide.
  • a solvent for example, dimethyl formamide, tetrahydrofuran, dioxane, diethyl ether, dichloromethane, toluene or dichloroethene
  • a base for example, potassium carbonate, triethylamine, N,N-diisopropylethylamine or N-methylmorpholine, optionally in the presence of a catalyst, like sodium iodide and
  • the compound of Formula XII can also be prepared, for example, following Scheme IV.
  • the compound of Formula X is reacted with a compound of Formula XIII (wherein Rp is alkyl or aryl) to form a compound of Formula XIV.
  • the compound of Formula XIV can be reacted with the compound of Formula VI to give a compound of Formula XV, which can be deprotected to give a compound of Formula XII.
  • the conversion of the compound of Formula X to the compound of Formula XIV can be carried out in three steps: 1) coupling of compounds of Formula X and Formula XIII in a solvent, for example, tetrahydrofuran, dimethyl formamide or dioxane, in the presence of a base, for example, potassium carbonate, triethylamine, NN- diisopropylethylamine or N-methylmorpholine; 2) protection of amine as, for example, t- butyl carbamate (Boc), 9-fluorenylmethyl carbamate (Fmoc), allyloxycarbonyl, or benzyl derivative using conditions available to the person skilled in the art of organic synthesis; and (3) hydrolysis with a base, for example, sodium hydroxide, potassium hydroxide or lithium hydroxide in a solvent, for example, ethanol, methanol, water, tetrahydrofuran or mixtures thereof.
  • a base for example, sodium hydroxide, potassium hydroxide or
  • the reaction of a compound of Formula XTV with the compound of Formula VT to give a compound of Formula XV can be carried out under similar conditions as that of the reaction of the compound of Formula VT with the compound of Formula VTI to form a compound of Formula VTII.
  • the deprotection of the compound of Formula XV to give the compound of Formula XII (Formula Ic) can be carried out under similar conditions as that of the deprotection of the compound of Formula Va to provide the compound of Formula VI.
  • the compound of Formula XII, wherein W is -CH 2 - can be prepared, for example, following Scheme V.
  • the compound of Formula XVT (can be prepared, for example, as described in WO 2004/103993) can be reacted with the compound of Formula VT in a solvent, for example, dichloromethane, to provide an intermediate, which, in turn, can be coupled with A-H (wherein A is defined as earlier) in the presence of an amino acid coupling agent (e.g., DCC, EDCI, etc.) and optionally a catalyst (e.g., HOBt) and an organic base (e.g., N-memylmorpholine) in a solvent, for example, dimethylformamide to give a compound of Formula XV, which, in turn, can be deprotected to give the compound of Formula XII.
  • a solvent for example, dichloromethane
  • the deprotection of the compound of Formula XV to give the compound of Formula XII can be carried out under similar conditions as that of the deprotection of the compound of Formula Va to provide the compound of Formula VT.
  • Step b Synthesis of phenyl ⁇ -amino-S-azabicyclop.l.Olhexane-S-carboxylate (pTSA salt)
  • Step a Synthesis of tot-butyl [3-(5-trifluoropyridin-2-yl)-3-azabicyclo[3.1.0]hex-6- yl] carbamate
  • Step b Synthesis of 3-[5-(trifluoromethyl)pyridin-2-yl]-3-azabicycIo[3.1.0]hexan-6- amine (pTSA salt)
  • Step a Synthesis oftert-butyl (3- ⁇ [(4-fluorophenyl)amino]carbonyl ⁇ -3- azabicyclo[3.1.0]hex-6-yl)carbamate
  • Step b Synthesis of 6-amino-iV-(4-fluorophenyl)-3-azabicycIo[3.1.0]hexane-3- carboxamide (pTSA salt)
  • reaction mixture was allowed to cool to room temperature and then partitioned between water (20.0 mL) and ether (20.0 mL). The organic layer was washed with brine, dried over anhydrous sodium sulphate and concentrated under reduced pressure to yield the residue, which was partially purified by column chromatography (silica gel 100-200 mesh, 25% ethyl acetate in hexane).
  • Step a Synthesis of tert-b ⁇ tyl [3-(4- ⁇ [(4-methylphenyl)sulphonyl]amino ⁇ phenyl)-3- azabicyclo[3.1.0]hex-6-yl] carbamate
  • 4-fluoroaniline 1.0 g, 9.0 mmol
  • triethylamine 1.32 g, 18.0 mmol
  • DCM 25.0 mL
  • the mixture was diluted with DCM (25.0 mL), washed with water and brine, dried over anhydrous sodium sulphate and concentrated in vacuo.
  • the crude product (1.50 g, 5.66 mmol), obtained, was mixed with tert-butyl 3-azabicyclo[3.1.0]hex-6-ylcarbamate (1.35 g, 6.79 mmol), and potassium carbonate (1.56 g, 11.32 mmol) in DMF (5.0 mL) and heated at 130 0 C overnight.
  • the mixture was partitioned between water (30.0 mL) and ethyl acetate (30.0 mL).
  • Step a Synthesis of (2.S',4»S',55)-iV-(te ⁇ -butyloxycarbonyl)-4,5-methanopyrrolidine-2- carbonitrile
  • (2 ⁇ S r ,46 r ,5,S)-N-(ter ⁇ -butyloxycarbonyl)-4,5-methanopyrrolidine-2- carboxamide 5.0 g, 22.09 mmol
  • trifluoroacetic anhydride (12.3 mL, 88.3 mmol
  • Step a Synthesis of ethyl 4-[(4-fluorobenzoyl)amino]benzoate
  • Step b Synthesis of 4-[(4-fluorobenzoyl)amino]benzoic acid
  • a solution of ethyl 4-[(4-fluorobenzoyl)amino]benzoate (0.700 g, 2.44 mmol) in the mixture of tetrahydrofuran and methanol (10.0 ml, 3:2)
  • aqueous solution of lithium hydroxide [2.0 mL] (0.153 g, 3.66 mmol
  • Step c Synthesis of fers-butyl (3- ⁇ 4-[(4-fluorobenzoyl)amino]benzoyl ⁇ 3- azabicyclo[3.1.0]hex-6-yl)carbamate
  • the reaction mixture was stirred at room temperature for about 16 hours and then partitioned between water (10.0 mL) and dichloromethane (15.0 mL). The aqueous layer was extracted with dichloromethane (15.0 mL). The combined organic layer was washed water and brine, dried over anhydrous sodium sulphate and concentrated under reduced pressure. The residue was purified by column chromatography (30% ethyl acetate in hexane, silica gel 100-200 mesh) to yield the title compound (792 mg, 85%).
  • Step d Synthesis of iV- ⁇ 4-[(6-amino-3-azabicyclo[3.1.0]hex-3-yl)carbonyl]phenyI ⁇ -4- fluorobenzamide (pTSA)
  • acetonitrile 7.0 mL
  • £>-toluenesulphonic acid 453 mg, 2.38 mmol
  • the reaction mixture was stirred for 12 h.
  • the solvent was evaporated and the crude mixture taken in ethyl acetate and stirred for 30 minutes.
  • the precipitate was filtered, washed with cold ethyl acetate and dried under reduced pressure to yield the title compound (530 mg, 65%)
  • reaction mixture was partitioned between water (10.0 mL) and dichloromethane (15.0 mL). The organic layer was washed with water and brine, dried over anhydrous sodium sulphate and concentrated under reduced pressure. The residue, obtained, was purified by column chromatography using 2% methanol in dichloromethane as eluant (silica gel 100- 200 mesh) to yield the title compound (40 mg, 23%).
  • Example 8 The following illustrative compounds were prepared by following one of the procedures of Example 8, Example 9 and Example 10 by coupling appropriate 3 -N- substituted-3 -azabicyclo[3.1.0]hexan-6-amine with (2S)- 1 -(chloroacetyl)pyrrolidine-2- carbonitrile or its derivative or thiazolidine:
  • Step a Synthesis of tert-butyl (2- ⁇ [3-(4-fluorobenzoyl)-3-azabicyclo[3.1.0]hex-6- yl]amino ⁇ -2-oxoethyl)carbamate
  • the reaction mixture was stirred at 0 0 C for about 1 hour followed by overnight at room temperature.
  • the precipitate was filtered and the filtrate diluted with ethylacetate, washed with water, aqueous citric acid (10%), water, aqueous sodium bicarbonate (10%), water and brine.
  • the organic layer was dried over anhydrous sodium sulphate, and concentrated under reduced pressure.
  • the residue, obtained, was purified by column chromatography using 10% methanol in dichloromethane as eluant (silica gel 100- 200 mesh) to yield the title compound (610.0 mg, 63%).
  • Step b Synthesis of iV-[3-(4-fluorobenzoyl)-3-azabicyclo[3.1.0]hex-6-yl]glycinamide (pTSA salt)
  • pTSA salt a compound obtained from step a in acetonitrile (10.0 mL)
  • /j-toluenesulphonic acid 0.474 g, 2.4 mmol
  • the mixture was stirred for about 24 hours at room temperature.
  • the solvent was evaporated and the residue taken in ethyl acetate and cooled to 0 0 C.
  • the precipitate was filtered, washed with cold ethyl acetate and dried to yield the title compound as colourless solid (0.620 g, 54%).
  • Step c Synthesis of (25)- ⁇ - ⁇ 2-[2-cyanopyrrolidin-l-yl]-2-oxoethyl ⁇ - ⁇ -[3-(4- fluorobenzoyl) -3-azabicyclo [3.1.0]hex-6-yl]glycinamide
  • compound (234 mg, 0.52 mmol) obtained from step b in anhydrous dimethylformamide (2.0 mL) under N 2 atmosphere at room temperature was added potassium carbonate (100 mg) and a solution of (2 ⁇ S)-l-(chloroacetyl)pyrrolidine-2- carbonitrile (75 mg, 0.43 mmol) in dimethylformamide (2.0 mL).
  • Example 12 Synthesis of (26'.46'.56 n )-l-IN-r3-f4-Methylbenzoyl)-3-azabicvclor3.1.01hex- 6-vHglvcyl
  • reaction mixture was stirred overnight at room temperature; diluted with dichloromethane (25 ml) and washed with water, brine and dried over anhydrous sodium sulphate and concentrated under vacuum to obtain the crude product that was purified by column chromatography using 2% methanol in dichloromethane as eluant (silica gel 100-200 mesh) to yield the title compound. (210 mg, 64%).
  • Step b Synthesis of (2£4£55)-l-(iV- ⁇ 3-[(4-fluorophenyl)carbonyl]-3- azabicycIo[3.1.0]hex-6-yI ⁇ gIycyl)-4,5-methanoproline-2-carbonitriIe
  • H-Gly-Pro-7-amido-methylcoumarine (Gly-Pro-AMC; Cat. # G2761) and coumarine (AMC; Cat. # A9891) were purchased from Sigma.
  • a stock solution of 1 mM Gly-Pro-AMC was prepared in 50 mM HEPES buffer, pH 7.8, containing 80 mM MgCl 2 , 140 mM NaCl and 1% BSA (working buffer).
  • a solution of 1 mM AMC was prepared in 10% dimethylsulfoxide (DMSO). Aliquots were stored at -20 0 C.
  • DPP IV Assay The DPP IV enzyme activity was determined using the fiuorometric assay with the substrate Gly-Pro-AMC, which is cleaved by DPP W to release the fluorescent AMC leaving group.
  • the test compounds were dissolved in 100% dimethylsulfoxide to get a final concentration of 10 mM.
  • the compounds were diluted serially in 10% DMSO to get 1OX concentrations of 10 nM, 100 nM, 1000 nM, 10 ⁇ M, 100 ⁇ M, and 1000 ⁇ M.
  • the source of DPP IV was human plasma, which was procured from local blood bank.
  • DPP IV (10 ⁇ l human plasma) was mixed in 96-well FluoroNunc plates with test compounds.
  • the final concentrations of the compounds were 1 nM, 10 nM, 100 nM, 1000 nM, 10 ⁇ M and 100 ⁇ M in working buffer, which were pre-incubated at 25 0 C for 15 min.
  • the assay was also carried out with 1% DMSO (final concentration), lacking the compound, as vehicle control.
  • the reaction was started by adding 20 ⁇ l of 0.1 mM H-Gly-Pro-AMC (40 ⁇ M final concentration), followed by mixing and incubation at 25 0 C for 20 min.
  • the reaction was arrested by adding 50 ⁇ l of 25% acetic acid.
  • the fluorescence was measured at an excitation filter of 380 nM and emission filter of 460 nM.
  • the DPP rv releases AMC from Gly-Pro-AMC, which was quantitated as relative fluorescence units (RFU).
  • REU relative fluorescence units
  • the ICs 0 is defined as the concentration of the inhibitor required to inhibit 50% of the human DPP IV activity under specific assay conditions.
  • the activity obtained at different concentrations of the compound was plotted as log (X) vs. % activity in y-axis.
  • the IC 50 values were calculated using non-linear regression analysis (GradPad Prism4).

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Abstract

La présente invention concerne des nouveaux dérivés de 3-azabicyclo[3.1.0]hexane en tant qu'inhibiteurs de la dipeptidyl peptidase-IV et les processus de synthèse desdits composés. Elle concerne également des compositions pharmaceutiques renfermant ces composés et des méthodes de traitement du diabète, en particulier du diabète de type 2, ainsi que du prédiabète, de la dyslipidémie diabétique, de l'acidose métabolique, de la cétose, des troubles de la satiété et de l'obésité. On peut utiliser également ces inhibiteurs pour le traitement de pathologies qui se manifestent par divers troubles métaboliques, neurologiques, anti-inflammatoires et auto-immunes tels que maladies inflammatoires, sclérose en plaques, polyarthrite rhumatoïde, troubles d'origine virale, cancéreuse et gastro-intestinale. Les composés de l'invention peuvent être également utilisés pour le traitement de la stérilité due à un syndrome des ovaires polykystiques.
EP06820744A 2005-09-05 2006-09-01 Derives de 3-azabicyclo[3.1.0]hexane en tant qu'inhibiteurs de la dipeptidyl peptidase-iv Withdrawn EP1931633A2 (fr)

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